Literature DB >> 27656430

Association of Salivary Osteopontin Levels with Glycaemic Status and Microalbuminuria - in Patients with Type 2 Diabetes Mellitus.

Niranjan Gopal1, Reeta Rajagambeeram2, Shruthi Venkatkumar3, Mohana Valli Vijayan4, Sathish Babu Murugaiyan2, Shyam Prakash Gopal5, Sathiya Ramsamy4, Velayutharaj Alwar6.   

Abstract

INTRODUCTION: The monitoring of glycaemic status in patients with T2DM is mainly through blood tests (Fasting plasma glucose and HbA1c), which are invasive and involves painful pricks. This leads to poor patient compliance and soon could lead to various micro and macro vascular complications, which hamper the quality of life. There are no sensitive and specific markers to predict these complications at the earliest. Sialochemistry has recently gained attention for monitoring chronic diseases. Osteopontin is a phospho-glycoprotein molecule, elevated in many inflammatory conditions. AIM: The aim of the study was to evaluate the role of serum and salivary osteopontin in Type 2 Diabetes mellitus (T2DM).
MATERIALS AND METHODS: In this case-control study, we recruited 33 cases of T2DM and 31 age and gender matched healthy controls. Body Mass Index (BMI), Waist/Hip Ratio (WHR), Waist Circumference (WC) and blood pressure was recorded. Fasting Plasma Glucose (FPG), salivary glucose, HbA1c, microalbuminuria, systolic BP, serum and salivary osteopontin levels were estimated.
RESULTS: FPG, salivary glucose, HbA1c, microalbuminuria, systolic BP, BMI, waist / hip ratio serum and salivary osteopontin levels were significantly high in T2DM cases compared to control subjects. Serum and salivary osteopontin levels were significantly correlated with HbA1c and microalbuminuria in T2DM cases.
CONCLUSION: Serum and salivary osteopontin levels are significantly elevated in subjects with T2DM and are associated with glycaemic control and microalbuminuria.

Entities:  

Keywords:  Diabetic nephropathy; Fasting Plasma Glucose; HbA1c

Year:  2016        PMID: 27656430      PMCID: PMC5028573          DOI: 10.7860/JCDR/2016/20156.8257

Source DB:  PubMed          Journal:  J Clin Diagn Res        ISSN: 0973-709X


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